Taiwan FDA registration 8fbf578bddf4c737a0585c86fffde9dd
“Philips” Avalon Fetal Monitor
TW: “飛利浦” 胎兒監視器
Taiwan·Risk Class 2·MD·PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH·Registered Mar 30, 2021 – Mar 30, 2026ExpiredRegistration details
- Analysis ID
- 8fbf578bddf4c737a0585c86fffde9dd
- License Form
- Ministry of Health Medical Device Import No. 034477
- Customs Code
- DHA05603447703
Company information
- Manufacturer
- PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L2740 Pre- and post-production monitoring system and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 30, 2021
- Expiry Date
- Mar 30, 2026
About this record
Access comprehensive regulatory information for “Philips” Avalon Fetal Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8fbf578bddf4c737a0585c86fffde9dd and manufactured by PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices